Figure 1. (click to enlarge) Effect of temperature on seal strength. The green bars represent samples created using low temperature. The orange indicates packages created using the high-temperature ...

In order to assist manufacturers in complying with the ISO 11607 standard requirements for packaging process development, equipment manufacturers are increasingly incorporating validation software and ...

Maintaining a healthy quality system and complying with the Food and Drug Administration’s expectations has never been more important for manufacturers making medical devices bound for the US market.

From my product development experiences, entering into Design Verification and Design Validation is always bittersweet. Exciting because yes, to get to Design Verification means that we have ...

Packaging for pharmaceutical products is aimed as to ensure that medicines arrive safely in the hands of the patients for whom they are prescribed. Manufacture of pharmaceutical products, quality ...

Green Bay, Wisconsin, March 01, 2022 (GLOBE NEWSWIRE) -- Green Bay Packaging announced today that the Green Bay mill achieved Net-Zero Water in its production of 100% recycled containerboard paper, ...

Sterilization is, of course, a fundamental requirement in the medical field. Here are four common reasons for failing a sterile barrier packaging validation test, presented by MDDI Online. 1.

Though it is widely understood that medical devices are developed under rigorous quality controls, it is less widely known that the packages that house them are also subjected to rigorous validation ...

Ideal for busy eCommerce Fulfillment Centers - PackVIEW is Engineered to improve outgoing order quality, PackVIEW also provides real-time goods fulfillment feedback and historical photographic records ...

Powertech Technology Inc (PTI) has gained validation from Toshiba for handset-use flash ball grid array (BGA) packaging, with volume shipments slated for February, according to the memory testing and ...